雑誌文献を検索します。書籍を検索する際には「書籍検索」を選択してください。

検索

書誌情報 詳細検索 by 医中誌

Japanese

Cerebellar Atrophy and Persistent Cerebellar Ataxia after Acute Intoxication of Phenytoin Toru Imamura 1 , Akiko Ejima 1 , Masaki Sahara 1 , Hiroshi Saito 1 , Kenji Tsuburaya 2 1Department of Neurology, Institute of Brain Diseases, Tohoku University School of Medicine 2Department of Neurology, Tohoku Kohseinenkin Hospital Keyword: phenytoin , acute intoxication , cerebellar atrophy , cerebellar ataxia , computed tomography pp.149-153
Published Date 1992/2/1
DOI https://doi.org/10.11477/mf.1406900299
  • Abstract
  • Look Inside

Chronic intoxication of phenytoin (PHT) is a well known cause of cerebellar atrophy or irrever-sible cerebellar ataxia. Little attention, on the other hand, is paid for acute PHT intoxication because its clinical signs are believed to be reversible. We here report a patient with acute PHT intoxication, which resulted in irreversible cerebellar ataxia with radiologically definite cerebellar atrophy.

A 39-year-old man admitted to our hospital because of cerebellar ataxia and confusional state. He had been treated with PHT for convulsive sei-zures after receiving craniotomy for left parietal brain abscess 9 years before. The concentration of his serum PHT had been 4 to 7μg/ml because he had frequently omitted taking drug, and the dose of PHT had been increased to 600 mg/day one year before. He had admitted to another hospital 2 months before for left Bell's palsy and had been obliged to take drug regularly. Cerebellar signs andconfusion had gradually developed for 7 weeks. On admission to our hospital, he was awake but in severe confusional state with slurred speech and nystagmus. His serum PHT was 86μg/ml, which returned to therapeutic range 2 weeks after the discontinuation of PHT. His consciousness normal-ized and nystagmus disappeared. However, slurred speech continued and neurological examination revealed postural tremor and severe limb ataxia. During the subsequent 10 months, his cerebellar signs showed minimal improvement. Computed tomographies of his brain on 3rd and 5th month after the onset of his cerebellar dysfunction showed the definite cerebellar atrophy which had not been noted on the CTs 7 months before and 7 weeks after the onset.

Our present observation and a review of literature suggested that not only chronic medication or into-xication of PHT but also several weeks of severe acute intoxication may resulted in irreversible cere-bellar degeneration and ataxia. Thus, we empha-size the underestimated harmfullness of acute PHT intoxication in clinical practice.


Copyright © 1992, Igaku-Shoin Ltd. All rights reserved.

基本情報

電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

関連文献

もっと見る

文献を共有